Product Details

SNP ID
rs77178633
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:48343734 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAAGAGCAGAGTCAGAGGTATTTG[C/T]AACTCTCAGGAAGATTTGAGTAACA
Phenotype
MIM: 610492
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLAIN2 PubMed Links

Gene Details

Gene
SLAIN2
Gene Name
SLAIN motif family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020846.1 Intron NP_065897.1
XM_005248121.2 Intron XP_005248178.1

View Full Product Details